Canonical Allele Identifier: CA470400652
Gene: IMPDH1P5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.79540836G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781078G>C , CM000672.2:g.77781078G>C GRCh38
NC_000010.10:g.79540836G>C , CM000672.1:g.79540836G>C GRCh37
NC_000010.9:g.79210842G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000439688.1:n.799C>G